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Fellowship - Real World Evidence / Clinical Data Science & Evidence

Employer
Novo Nordisk
Location
Plainsboro, NJ
Start date
Dec 13, 2024
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Job Details

About the Department                                                                                                                                               

The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the same beat is our patient-centered focus. At Novo Nordisk, you will help patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We’re changing lives for a living. Are you ready to make a difference?

 

The Position
The Novo Nordisk Real World Evidence (RWE) / Clinical Data Science & Evidence (CDSE) - Fellow is responsible for supporting planning and execution of observational research / Real World Evidence studies to support the Evidence and Insights Generation Plans (EIGPs) for specific areas of the Novo Nordisk portfolio. In addition, the incumbent may also coordinate other activities including but not limited to cross-functional team meetings, project team meetings and observational study protocol reviews. One of the key responsibilities for the fellow is leading specific research studies, as identified during the annual EIGP process to support the product strategy; the Fellow may also be involved in activities surrounding study execution, for example supporting the communication of study results across the organization. This is an experiential fellowship, and the fellow will gain valuable experience in observing the development of product strategy, engaging with cross functional teams, leading research projects, coordinating/managing research vendors, & budget management. 


Relationships
The fellow will report to the Senior Director RWE during the program and will work closely with all colleagues in both the RWE and the broader CDSE department. 


Essential Functions

  • Lead observational research projects and manage vendors, contracts and budget.
  • Interact with cross functional internal stakeholders as part of research projects.
  • Prepare protocols for internal approvals and engage reviewers during approval process.
  • Responsible for data dissemination for specific research projects – includes external and internal stakeholders, managing the publication planning process.
  • Work in close collaboration with colleagues within the CDSE team and also broader stakeholders across Novo Nordisk Inc for example Medical, Market Access, etc.
  • Communication and training of HEOR content.
  • Be involved, as appropriate, in broader initiatives executed through the CDSE department to further support the processes and development of RWE.
  • Throughout the fellowship the Fellow will also be expected to develop and publish a post-doc project; the RWD available to Novo Nordisk Inc will be available to support this project which will be anchored in the broader EIGP.


Physical Requirements

  • Approximately 10% overnight travel.


Qualifications

  • A PhD (either completed or ABD), in appropriate field of heath economics, epidemiology, outcomes research, public health, or health services research.
  • Strong academic track record preferred.
  • Demonstrated leadership capabilities.
  • Presentable, highly articulate, goal-oriented, honest, with high integrity and strong ethics.
  • Track record of teamwork, innovation and project management.
  • Ability to think critically, strategically, and independently.
  • Possess good communication skills, both oral, written and presentation.
  • Demonstrate an ability to perform medical accuracy review with strong attention to detail.
  • Proficiency in Microsoft Office software applications such as PowerPoint, Excel and Word and overall computer skills with knowledge of literature search technique required.

 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

 

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

 

Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

 

If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

Company

Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat diabetes and other serious chronic diseases such as obesity and rare blood and endocrine disorders. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 54,400 people in 80 countries and markets its products in around 170 countries. For more information visit novonordisk.com.

Our US Research & Development hub, located in the Greater Boston area, brings together the best talent to drive life science innovation. Located in Lexington, Watertown and Cambridge, our teams reflect the full scope of R&D, from early research through late-stage clinical development. We are building for the future by creating a distinct R&D community based on collaboration, partnerships, and cutting-edge research across multiple modalities and therapeutic areas. We recognize that improving human health starts here and that patients rely on us. By combining the speed and agility of biotech with the quality, resources, and stability of a large pharmaceutical company, our US R&D hub will benefit from the best of both worlds to develop new medicines that meet the needs of patients.

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Company info
Website
Phone
617-612-6200
Location
75 Hayden Avenue
Lexington
MA
02421
United States

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